Figure 2
Figure 2. Osteopoietic chimerism and histomorphometry. (A) Osteoblast (OB) chimerism, determined by immunohistochemical staining for GFP expression, in the epiphysis (left) and metaphysis (right) at 1 and 4 weeks after cytokine treatment. n = 5 for each cytokine group at each time point; 8 sections per mouse were analyzed. (B) Histomorphometric analyses of bone from G-CSF–, GH-, and saline-treated mice obtained at 1 (left) and 4 (right) weeks after completion of the cytokine regimen. n = 5 for each cytokine group. (C) Osteocyte (OC) chimerism, determined by immunohistochemical staining for GFP expression, in the epiphysis (left) and metaphysis (right) at 1 and 4 weeks after cytokine treatment. n = 5 for each cytokine group at each time point; 8 sections per mouse. All data are presented as mean ± SE. Statistically significant relationships are indicated. ***P < .001, **P < .01, and *P < .05 compared with saline group at the same time point.

Osteopoietic chimerism and histomorphometry. (A) Osteoblast (OB) chimerism, determined by immunohistochemical staining for GFP expression, in the epiphysis (left) and metaphysis (right) at 1 and 4 weeks after cytokine treatment. n = 5 for each cytokine group at each time point; 8 sections per mouse were analyzed. (B) Histomorphometric analyses of bone from G-CSF–, GH-, and saline-treated mice obtained at 1 (left) and 4 (right) weeks after completion of the cytokine regimen. n = 5 for each cytokine group. (C) Osteocyte (OC) chimerism, determined by immunohistochemical staining for GFP expression, in the epiphysis (left) and metaphysis (right) at 1 and 4 weeks after cytokine treatment. n = 5 for each cytokine group at each time point; 8 sections per mouse. All data are presented as mean ± SE. Statistically significant relationships are indicated. ***P < .001, **P < .01, and *P < .05 compared with saline group at the same time point.

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